May 1986

The Conundrum of Cushing's Syndrome

Author Affiliations

Department of Internal Medicine Division of Endocrinology Henry Ford Hospital 2799 W Grand Blvd Detroit, MI 48202

Arch Intern Med. 1986;146(5):858-860. doi:10.1001/archinte.1986.00360170054004

Cushing's syndrome has presented clinicians with fascinating diagnostic and therapeutic difficulties for more than half a century. Additional causative mechanisms and different means of treatment continue to be advanced. Although the syndrome usually results from a disordered function originating in the pituitary or the adrenal glands, pathologic hypercortisolism is also well known to result from ectopic secretions. The ectopic corticotropin (ACTH) syndrome, which is characteristic of the latter disorders, is usually associated with very high levels of ACTH secretion, great excesses of cortisol, bilateral adrenal hypertrophy, pigmentation, hypokalemia, hyperglycemia, and hypertension. The very high levels of cortisol accelerate the pace of the disorder, and the underlying malignancy modifies the clinical expression of the endocrine disease. Instead of a classically obese, plethoric patient with Cushing's syndrome, victims are usually severely wasted.1 In his 1979 review of the Cushing syndromes, Gold2 proposed a useful diagnostic algorithm that integrated ACTH assays

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